rs121909665

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121909665(A;A)

Make rs121909665(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

48990629

Gene

FSHR

is a	snp
is	mentioned by
dbSNP	rs121909665
dbSNP (classic)	rs121909665
ClinGen	rs121909665
ebi	rs121909665
HLI	rs121909665
Exac	rs121909665
Gnomad	rs121909665
Varsome	rs121909665
LitVar	rs121909665
Map	rs121909665
PheGenI	rs121909665
Biobank	rs121909665
1000 genomes	rs121909665
hgdp	rs121909665
ensembl	rs121909665
geneview	rs121909665
scholar	rs121909665
google	rs121909665
pharmgkb	rs121909665
gwascentral	rs121909665
openSNP	rs121909665
23andMe	rs121909665
SNPshot	rs121909665
SNPdbe	rs121909665
MSV3d	rs121909665
GWAS Ctlg	rs121909665

Max Magnitude

0

OMIM	136435
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121909665(A;A)
Alt	rs121909665(A;A)
Reference	Rs121909665(C;C)
Significance	Pathogenic
Disease	Ovarian hyperstimulation syndrome
Variation	info
Gene	FSHR
CLNDBN	Ovarian hyperstimulation syndrome
Reversed	1
HGVS	NC_000002.11:g.49217768G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017642.24,